|
amelogenesis imperfecta and nephrocalcinosis
|
8771 |
|
|
interventricular septum congenital heart malformation
|
18771 |
|
|
amelogenesis imperfecta caused by mutation in FAM20A
|
8771 |
|
|
generalized enamel hypoplasia and renal dysfunction
|
8771 |
|
|
amelogenesis imperfecta hypoplastic type, IG
|
8771 |
|
|
amelogenesis imperfecta-gingival hyperplasia syndrome
|
8771 |
|
|
amelogenesis imperfecta hypoplastic type, Ig
|
http://purl.obolibrary.org/obo/MONDO_0008771 |
|
|
amelogenesis imperfecta hypoplastic with nephrocalcinosis
|
8771 |
|
|
amelogenesis imperfecta, hypoplastic, with nephrocalcinosis
|
8771 |
|
|
congenital anomaly of interventricular communication
|
18771 |
|
|
FAM20A amelogenesis imperfecta
|
8771 |
|
|
congenital heart malformation of interventricular septum
|
18771 |
|
|
amelogenesis imperfecta nephrocalcinosis
|
8771 |
|
|
absent enamel, nephrocalcinosis and apparently normal calcium metabolism
|
8771 |
|
|
amelogenesis imperfecta-nephrocalcinosis syndrome
|
8771 |
|
